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โ† Trials
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Efficacy and Safety of GNT0003 Following Imlifidase Pre-treatment in Severe Crigler-Najjar Syndrome

RecruitingPhase 2Ages 18 Years - anyAllGenethon
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In plain words

What the trial is, and whether it could suit you

Clinical trial rationale: CNS is an ultra-rare (\<1/1 million newborns), autosomal recessive disorder of bilirubin conjugation caused by mutation in the gene coding for uridine 5'-diphosphate glucuronosyltransferase (UGT1A1), that causes the accumulation of neurotoxic unconjugated bilirubin (UCB). Reduction of UCB is managed with phenobarbital in mild CNS, and daily phototherapy in severe CNS. There is no authorized curative medical treatment for CNS. Liver transplantation is currently the only curative treatment for severe CNS. GNT0003 is a genetically modified recombinant (r) viral vector composed of the AAV8 viral capsid carrying the UGT1A1 transgene which aims to correct the dysfunction of the mutated gene by achieving durable expression of a functional copy of the affected gene. Imlifidase (IgG-degrading enzyme) has demonstrated its efficacy in highly sensitized adult kidney tr

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Main Inclusion Criteria: 1. Severe Crigler-Najjar syndrome requiring โ‰ฅ 6 hours/ day of phototherapy 2. Molecular confirmation of mutation in the UGT1A1gene by DNA sequencing 3. Detectable serum neutralizing antibodies against AAV8 4. Laboratory parameters value not clinically significant 5. Highly effective method of contraception 6. Affiliated to or a beneficiary of a health care system Exclusion Criteria: 1. Participation in another interventional trial within 6 months prior to start of clinical trial intervention and during the whole clinical trial 2. Fibrosis score โ‰ฅ 3 (METAVIR) or 10 kPa (FibroScanยฎ) 3. Liver transplantation 4. Significant underlying liver disease, chronic hepatitis B, C and/or infected with Human immunodeficiency virus 5. Any other clinically significant illness 6. Uncontrolled hyperlipidemia. 7. History of major thrombotic events, active peripheral vascular disease, proven hypercoagulable conditions, 8. History or presence of thrombotic thrombocytopenic purpura (TTP) or known familial history of TTP 9. Prior or current treatment with Gene therapy, cell based therapy, CRISPR/Cas9 or any other form of gene editing, imlifidase
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What it tests

  • Imlifidase
  • GNT0003
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Where

1 site
Hopital Antoine BECLERE
Clamart, France
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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